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Rexall Pain Relief
Rexall Pain Relief - 55910-703-82 - (Acetaminophen)
Drug Information of Rexall Pain Relief
| Product NDC: | 55910-703 |
| Proprietary Name: | Rexall Pain Relief |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rexall Pain Relief
| Product NDC: | 55910-703 |
| Labeler Name: | Dolgencorp, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100921 |
Package Information of Rexall Pain Relief
| Package NDC: | 55910-703-82 |
| Package Description: | 1 BOTTLE in 1 CARTON (55910-703-82) > 200 TABLET in 1 BOTTLE |
NDC Information of Rexall Pain Relief
| NDC Code | 55910-703-82 |
| Proprietary Name | Rexall Pain Relief |
| Package Description | 1 BOTTLE in 1 CARTON (55910-703-82) > 200 TABLET in 1 BOTTLE |
| Product NDC | 55910-703 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100921 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Dolgencorp, LLC |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
